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Revue Medicale De Liege|June 15, 2007
[Pathogenesis of Alzheimer's disease: molecular and cellular mechanisms]L Govaerts, J Schoenen, D BouhyTijdschrift Voor Kindergeneeskunde|August 1, 1985
[Peroxisomes--in search of their function in man]L Monnens, F Trijbels, L GovaertsJournal of Inherited Metabolic Disease|January 1, 1989
Further analysis of the disturbed adrenocortical function in the cerebro-hepato-renal syndrome of ZellwegerL Govaerts, W G Sippell, L MonnensEuropean Journal of Pediatrics|November 1, 1984
Disturbed adrenocortical function in cerebro-hepato-renal syndrome of ZellwegerL Govaerts, L Monnens, T Melis, et al.Neuropediatrics|November 1, 1985
A neurophysiological study of children with the cerebro-hepato-renal syndrome of ZellwegerL Govaerts, E Colon, J Rotteveel, et al.Annales De Genetique|January 1, 1996
Another patient with a deletion 14q11.2q13L Govaerts, J Toorman, M V Blij-Philipsen, et al.Journal of Inherited Metabolic Disease|January 1, 1985
Pipecolic acid levels in serum and urine from neonates and normal infants: comparison with values reported in Zellweger syndromeL Govaerts, F Trijbels, L Monnens, et al.Tijdschrift Voor Kindergeneeskunde|April 1, 1983
[A child with Zellweger's cerebrohepatorenal syndrome]L Govaerts, J Corstiaensen, J Bakkeren, et al.Cancer Genetics and Cytogenetics|February 1, 1988
Deletion (8)(q22) as the only chromosomal abnormality in a patient with RAEB-t with progression to acute myelocytic leukemiaL Govaerts, S Daenen, B Bong, et al.Prenatal Diagnosis|September 1, 1986
Abnormal karyotype in the chorion, not confirmed in a subsequently aborted fetusA Breed, A Mantingh, L Govaerts, et al.Pageof 2